Canonical Allele Identifier: CA1624127825

Gene: UBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42594238A= , CM000668.2:g.42594238A=	GRCh38
NC_000006.11:g.42561976A= , CM000668.1:g.42561976A=	GRCh37
NC_000006.10:g.42669954A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372899.6:c.465A=	ENSP00000361990.1:p.Glu155=
ENST00000372901.2:c.465A= MANE Select	ENSP00000361992.1:p.Glu155=
ENST00000372899.5:c.465A=	ENSP00000361990.1:p.Glu155=
ENST00000372901.1:c.465A=	ENSP00000361992.1:p.Glu155=
ENST00000372903.6:c.465A=	ENSP00000361994.2:p.Glu155=
NM_001184801.1:c.465A=	NP_001171730.1:p.Glu155=
NM_015255.2:c.465A=	NP_056070.1:p.Glu155=
XM_005248965.3:c.465A=	XP_005249022.1:p.Glu155=
XM_011514438.1:c.279A=	XP_011512740.1:p.Glu93=
XM_011514442.1:c.465A=	XP_011512744.1:p.Glu155=
NM_001363705.1:c.465A=	NP_001350634.1:p.Glu155=
XM_005248966.3:c.-1641A=	XP_005249023.1:n.-1641A=
XM_011514438.2:c.546A=	XP_011512740.2:p.Glu182=
XM_017010594.1:c.546A=	XP_016866083.1:p.Glu182=
XM_017010595.1:c.546A=	XP_016866084.1:p.Glu182=
XM_017010596.1:c.465A=	XP_016866085.1:p.Glu155=
XM_017010597.1:c.546A=	XP_016866086.1:p.Glu182=
XR_001743284.2:n.964A=
XR_001743285.1:n.965A=
NM_001184801.2:c.465A=	NP_001171730.1:p.Glu155=
NM_001363705.2:c.465A= MANE Select	NP_001350634.1:p.Glu155=
NM_015255.3:c.465A=	NP_056070.1:p.Glu155=